| Primary Device ID | 10859273007172 |
| NIH Device Record Key | 76d7bd8b-0e0f-4363-969c-4649aa016216 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Exoflow™ |
| Version Model Number | R-10017 |
| Catalog Number | R-10017 |
| Company DUNS | 080031617 |
| Company Name | RELIGN CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00859273007175 [Primary] |
| GS1 | 08592730070177 [Previous] |
| GS1 | 10859273007172 [Package] Contains: 00859273007175 Package: Shipper [6 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-28 |
| Device Publish Date | 2020-02-20 |
| 18592730070174 | Fluid management accessory disposable, outflow only |
| 10859273007172 | Fluid management accessory disposable, outflow only |